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The protein Gnαs is found more in black mice than white mice and may influence their coat color.

Monilethrix causes brittle hair and hair loss, and it runs in families.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

KLHL24-mutant stem cells help understand skin and heart disease.

A new genetic mutation causing Werner's syndrome was found in an Indian man.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

Phosphorylation of certain parts of the PIN3 protein is crucial for its role in plant root growth and response to gravity.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.

Mutations in hKAP1 genes may cause hereditary hair disorders.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Certain genetic variants increase the risk of aggressive prostate cancer.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

Diet changes can protect against harmful environmental effects on fetal development.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Minoxidil boosts hair growth in genetically modified mice.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

The Itpr3 gene causes a specific hair pattern in mice.

Blocking mTORC1 reduces skin tumor growth in mice.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.